Proliferation and migration of hepatocellular carcinoma are accelerated by LINC01287 via the miR-559/TCF12 axis.
Journal
European review for medical and pharmacological sciences
ISSN: 2284-0729
Titre abrégé: Eur Rev Med Pharmacol Sci
Pays: Italy
ID NLM: 9717360
Informations de publication
Date de publication:
06 2020
06 2020
Historique:
entrez:
24
6
2020
pubmed:
24
6
2020
medline:
22
4
2021
Statut:
ppublish
Résumé
To uncover the role of LINC01287 in the progression of hepatocellular carcinoma (HCC) and the indicated molecular mechanism. Relative levels of LINC01287 and miR-559 in 32 pairs of HCC tissues and normal ones, as well as HCC cell lines were detected by quantitative real-time polymerase chain reaction (qRT-PCR). Receiver operating characteristic (ROC) curves and Kaplan-Meier curves were depicted for assessing the diagnostic and prognostic potentials of LINC01287 in HCC, respectively. Proliferative and migratory capacities in HCC cells influenced by LINC01287 were assessed by cell counting kit-8 (CCK-8) and transwell assay, respectively. The regulatory loop LINC01287/miR-559/TCF12 was ascertained by Dual-Luciferase reporter assay. The involvement of the regulatory loop in the progression of HCC was examined via rescue experiments. LINC01287 was upregulated in HCC tissues and cell lines, whereas miR-559 was downregulated. LINC01287 displayed certain diagnostic and prognostic potentials in HCC. Knockdown of LINC01287 could inhibit proliferative and migratory capacities in HCC cells. The regulatory loop LINC01287/miR-559/TCF12 was responsible for the aggravation of HCC. LINC01287 drives proliferative and migratory capacities in HCC via targeting the miR-559/TCF12 axis.
Identifiants
pubmed: 32572916
doi: 10.26355/eurrev_202006_21496
pii:
doi:
Substances chimiques
Basic Helix-Loop-Helix Transcription Factors
0
MIRN559 microRNA, human
0
MicroRNAs
0
RNA, Long Noncoding
0
TCF12 protein, human
142661-93-6
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM